Absorbent article comprising a malodor control composition having an acid catalyst

ABSTRACT

An absorbent article comprising a malodor control composition having at least one volatile aldehyde and an acid catalyst, and methods of use thereof, are provided. The malodor control composition is suitable for a variety of absorbent articles, including use in diapers, toddler training pants, adult incontinence garments, sanitary napkins, pantiliners, interlabial devices, hemorrhoid pads, and the like.

CROSS REFERENCE TO RELATED APPLICATION

This application claims the benefit of U.S. patent application Ser. No.12/970,098, filed Dec. 16, 2010 which claims the benefit of U.S.Provisional Application No. 61/287,369, filed on Dec. 17, 2009; bothincorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to an absorbent article comprising amalodor control composition having at least one volatile aldehyde and anacid catalyst, and methods of use. The malodor control composition issuitable for use in a variety of absorbent articles, including diapers,toddler training pants, adult incontinence garments, sanitary napkins,pantiliners, interlabial devices, hemorrhoid pads, and the like.

BACKGROUND OF THE INVENTION

Products for reducing or masking malodors are well known in the art andare widely described in patent literature. These products may bedesigned to work specifically in air or on fabrics or other surfaces.See, e.g., U.S. Pat. Nos. 5,942,217; 5,955,093; and 6,033,679. However,not all odors are effectively controlled by products on the market, suchas amine-based malodors associated with urine and sulfur-based malodorsassociated with bodily fluids and excrements such as menses and feces,which are difficult to combat. Further, the time required for acomposition to noticeably combat malodors may create consumer doubt asto a product's efficacy on malodors. For example, the malodor may becomenoticeable to a consumer of the product before the product begins tonoticeably reduce the malodor.

In the context of absorbent articles, previous attempts have been madeto develop compositions for incorporation in absorbent article tocontrol malodor associated with bodily fluids and excrement, such asurine, menses, and feces. Some known malodor control compositionsprovide an overwhelming perfume scent to the product that may not beacceptable to some consumers. There thus still remains a desire toprovide an improved malodor control composition for incorporation intoan absorbent article product.

There remains a need for a fast acting malodor control composition thatneutralizes malodors and is effective on a broad range of malodors,including amine-based and sulfur-based malodors, while not overpoweringmalodors with an overwhelming perfume.

SUMMARY OF THE INVENTION

The present invention encompasses an absorbent article comprising amalodor control composition comprising at least one volatile aldehyde;and an acid catalyst having a vapor pressure of about 0.01 to about 13at 25° C.

The present invention further encompasses a method of neutralizingmalodor comprising contacting the malodor with a malodor controlcomposition comprising at least one volatile aldehyde; and an acidcatalyst having a vapor pressure of about 0.01 to about 13 at 25° C.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph showing butanethiol reduction by thiophenecarboxaldehyde in combination with various acid catalysts.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a malodor control composition having atleast one volatile aldehyde and an acid catalyst for neutralizingmalodors, and methods thereof.

“Malodor” refers to compounds generally offensive or unpleasant to mostpeople, such as the complex odors associated with bowel movements (i.e.feces) or other bodily excrements or fluids.

“Neutralize” or “neutralization” refers to the ability of a compound orproduct to reduce or eliminate malodorous compounds. Odor neutralizationmay be partial, affecting only some of the malodorous compounds in agiven context, or affecting only part of a malodorous compound. Amalodorous compound may be neutralized by chemical reaction resulting ina new chemical entity, by sequestration, by chelation, by association,or by any other interaction rendering the malodorous compound lessmalodorous or non-malodorous. Odor neutralization may be distinguishedfrom odor masking or odor blocking by a change in the malodorouscompound, as opposed to a change in the ability to perceive the malodorwithout any corresponding change in the condition of the malodorouscompound.

“Absorbent article” refers to devices that absorb and contain bodyexudates, such as urine, menses, and feces. The term “disposable” isused herein to describe absorbent articles which are not intended to belaundered or otherwise restored or reused as an absorbent article aftera single use. Examples of absorbent articles include diapers, toddlertraining pants, adult incontinence garments, and feminine hygienegarments such as sanitary napkins, pantiliners, interlabial devices,hemorrhoid pads, and the like.

Absorbent articles and components thereof, including the topsheet,backsheet, absorbent core, and any individual layers of thesecomponents, have a body surface and a garment surface. As used herein,“body surface” means that surface of the article or component which isintended to be worn toward or adjacent to the body of the wearer, whilethe “garment surface” is on the opposite side and is intended to be worntoward or placed adjacent to the wearer's undergarments when thedisposable absorbent article is worn.

I. Absorbent Article

In general, the absorbent articles of the present invention typicallycomprise a topsheet, a backsheet, and an absorbent core disposed betweenthe topsheet and backsheet.

The topsheet of the absorbent article is preferably compliant, softfeeling, and non-irritating to the wearers skin and hair. Further, thetopsheet is liquid pervious, permitting liquids (e.g., menses and/orurine) to readily penetrate through its thickness. A suitable topsheetmay be manufactured from a wide range of materials such as woven andnonwoven materials (e.g., a nonwoven web of fibers); polymeric materialssuch as apertured formed thermoplastic films, apertured plastic films,and hydroformed thermoplastic films; porous foams; reticulated foams;reticulated thermoplastic films; and thermoplastic scrims. Suitablewoven and nonwoven materials can be comprised of natural fibers (e.g.,wood or cotton fibers), synthetic fibers (e.g., polymeric fibers such aspolyester, polypropylene, or polyethylene fibers) or from a combinationof natural and synthetic fibers. When the topsheet comprises a nonwovenweb, the web may be manufactured by a wide number of known techniques.For example, the web may be spunbonded, carded, wet-laid, melt-blown,hydroentangled, combinations of the above, or the like.

The backsheet is impervious to liquids (e.g., menses and/or urine) andis preferably manufactured from a thin plastic film, although otherflexible liquid impervious materials may also be used. As used herein,the term “flexible” refers to materials which are compliant and willreadily conform to the general shape and contours of the human body. Thebacksheet prevents the exudates absorbed and contained in the absorbentcore from wetting articles which contact the absorbent article such asbedsheets, pants, pajamas and undergarments. The backsheet can also bevapor permeable (“breathable”), while remaining fluid impermeable. Thebacksheet may comprise a woven or nonwoven material, polymeric filmssuch as thermoplastic films of polyethylene or polypropylene, orcomposite materials such as a film-coated nonwoven material.

The backsheet and the topsheet can positioned adjacent the garmentsurface and the body surface, respectively, of the absorbent core. Theabsorbent core can be joined with the topsheet, the backsheet, or bothin any manner as is known by attachment means such as those well knownin the art. Embodiments of the present invention are envisioned whereinportions of the entire absorbent core are unattached to either thetopsheet, the backsheet, or both.

The absorbent core can be formed from any of the materials well known tothose of ordinary skill in the art. Examples of such materials includemultiple plies of creped cellulose wadding, fluffed cellulose fibers,wood pulp fibers also known as airfelt, textile fibers, a blend offibers, a mass or batt of fibers, airlaid webs of fibers, a web ofpolymeric fibers, and a blend of polymeric fibers.

For some absorbent articles, the absorbent core can be relatively thin,less than about 5 mm in thickness, or less than about 3 mm, or less thanabout 1 mm in thickness. Thickness can be determined by measuring thethickness at the midpoint along the longitudinal centerline of the padby any means known in the art for doing while under a uniform pressureof 1.72 kPa. The absorbent core can comprise superabsorbent materialssuch as absorbent gelling materials (AGM), including AGM fibers, as isknown in the art.

The absorbent article can comprise other additional components, forexample between the topsheet and absorbent core, such as a secondarytopsheet or acquisition layer. The secondary topsheet or acquisitionlayer can comprise a tissue layer or a nonwoven, such as cardedresin-bonded nonwovens, embossed carded resin-bonded nonwovens,high-loft carded resin-bonded nonwovens, carded through-air-bondednonwovens, carded thermo-bonded nonwovens, spunbonded nonwovens, and thelike. A variety of fibers can be used in the secondary topsheet oracquisition layer, including natural fibers, e.g. wood pulp, cotton,wool, and the like, as well as biodegradable fibers, such as polylacticacid fibers, and synthetic fibers such as polyolefins (e.g.,polyethylene and polypropylene), polyesters, polyamides, syntheticcellulosics (e.g., RAYON®, Lyocell), cellulose acetate, bicomponentfibers, and blends thereof. The basis weight of the secondary topsheetor acquisition layer can vary depending upon the desired application.

The absorbent article can comprise further components such as sidecuffs, typically found in diapers, or side wings or side flaps,typically found in sanitary napkins.

The absorbent articles herein are preferably disposable after a singleuse.

The malodor control composition of the present invention can be disposedin various locations in the absorbent article. The malodor controlcomposition can be disposed on the garment-facing side or thebody-facing side of the topsheet or absorbent core, or the body-facingside of the backsheet. Preferably, the malodor control composition isdisposed on the absorbent core, and preferably on the garment-facingside of the absorbent core. The malodor control composition can also bedisposed on other components, when present in the absorbent article,such as the garment-facing side or body-facing side of a secondarytopsheet or acquisition layer.

II. Malodor Control Composition

The malodor control composition includes a mixture of volatile aldehydesand is designed to deliver genuine malodor neutralization and notfunction merely by covering up or masking odors. A genuine malodorneutralization provides a sensory and analytically measurable (e.g. gaschromatograph) malodor reduction. Thus, if the malodor controlcomposition delivers a genuine malodor neutralization, the compositionwill reduce malodors in the vapor and/or liquid phase.

1. Volatile Aldehydes

The malodor control composition includes a mixture of volatile aldehydesthat neutralize malodors in vapor and/or liquid phase via chemicalreactions. Such volatile aldehydes are also called reactive aldehydes(RA). Volatile aldehydes may react with amine-based odors, following thepath of Schiff-base formation. Volatiles aldehydes may also react withsulfur-based odors, forming thiol acetals, hemi thiolacetals, and thiolesters in vapor and/or liquid phase. It may be desirable for these vaporand/or liquid phase volatile aldehydes to have virtually no negativeimpact on the desired perfume character of a product. Aldehydes that arepartially volatile may be considered a volatile aldehyde as used herein.

Suitable volatile aldehydes may have a vapor pressure (VP) in the rangeof about 0.0001 torr to 100 torr, alternatively about 0.0001 torr toabout 10 torr, alternatively about 0.001 torr to about 50 torr,alternatively about 0.001 torr to about 20 torr, alternatively about0.001 torr to about 0.100 torr, alternatively about 0.001 torr to 0.06torr, alternatively about 0.001 torr to 0.03 torr, alternatively about0.005 torr to about 20 torr, alternatively about 0.01 torr to about 20torr, alternatively about 0.01 torr to about 15 torr, alternativelyabout 0.01 torr to about 10 torr, alternatively about 0.05 torr to about10 torr, measured at 25° C.

The volatile aldehydes may also have a certain boiling point (B.P.) andoctanol/water partition coefficient (P). The boiling point referred toherein is measured under normal standard pressure of 760 mmHg. Theboiling points of many volatile aldehydes, at standard 760 mm Hg aregiven in, for example, “Perfume and Flavor Chemicals (Aroma Chemicals),”written and published by Steffen Arctander, 1969.

The octanol/water partition coefficient of a volatile aldehyde is theratio between its equilibrium concentrations in octanol and in water.The partition coefficients of the volatile aldehydes used in the malodorcontrol composition may be more conveniently given in the form of theirlogarithm to the base 10, logP. The logP values of many volatilealdehydes have been reported. See, e.g., the Pomona92 database,available from Daylight Chemical Information Systems, Inc. (DaylightCIS), Irvine, Calif. However, the logP values are most convenientlycalculated by the “CLOGP” program, also available from Daylight CIS.This program also lists experimental logP values when they are availablein the Pomona92 database. The “calculated logP” (ClogP) is determined bythe fragment approach of Hansch and Leo (cf., A. Leo, in ComprehensiveMedicinal Chemistry, Vol. 4, C. Hansch, P. G. Sammens, J. B. Taylor andC. A. Ramsden, Eds., p. 295, Pergamon Press, 1990). The fragmentapproach is based on the chemical structure of each volatile aldehyde,and takes into account the numbers and types of atoms, the atomconnectivity, and chemical bonding. The ClogP values, which are the mostreliable and widely used estimates for this physicochemical property,are preferably used instead of the experimental logP values in theselection of volatile aldehydes for the malodor control composition.

The ClogP values may be defined by four groups and the volatilealdehydes may be selected from one or more of these groups. The firstgroup comprises volatile aldehydes that have a B.P. of about 250° C. orless and ClogP of about 3 or less. The second group comprises volatilealdehydes that have a B.P. of 250° C. or less and ClogP of 3.0 or more.The third group comprises volatile aldehydes that have a B.P. of 250° C.or more and ClogP of 3.0 or less. The fourth group comprises volatilealdehydes that have a B.P. of 250° C. or more and ClogP of 3.0 or more.The malodor control composition may comprise any combination of volatilealdehydes from one or more of the ClogP groups.

In some embodiments, the malodor control composition of the presentinvention may comprise, by total weight of the malodor controlcomposition, from about 0% to about 30% of volatile aldehydes from group1, alternatively about 25%; and/or about 0% to about 10% of volatilealdehydes from group 2, alternatively about 10%; and/or from about 10%to about 30% of volatile aldehydes from group 3, alternatively about30%; and/or from about 35% to about 60% of volatile aldehydes from group4, alternatively about 35%.

Exemplary volatile aldehydes which may be used in a malodor controlcomposition include, but are not limited to, Adoxal(2,6,10-Trimethyl-9-undecenal), Bourgeonal(4-t-butylbenzenepropionaldehyde), Lilestralis 33(2-methyl-4-t-butylphenyl)propanal), Cinnamic aldehyde, cinnamaldehyde(phenyl propenal, 3-phenyl-2-propenal), Citral, Geranial, Neral(dimethyloctadienal, 3,7-dimethyl-2,6-octadien-1-al), Cyclal C(2,4-dimethyl-3-cyclohexen-1-carbaldehyde), Florhydral(3-(3-Isopropyl-phenyl)-butyraldehyde), Citronellal (3,7-dimethyl6-octenal), Cymal, cyclamen aldehyde, Cyclosal, Lime aldehyde(Alpha-methyl-p-isopropyl phenyl propyl aldehyde), Methyl NonylAcetaldehyde, aldehyde C12 MNA (2-methyl-1-undecanal),Hydroxycitronellal, citronellal hydrate (7-hydroxy-3,7-dimethyloctan-1-al), Helional(alpha-methyl-3,4-(methylenedioxy)-hydrocinnamaldehyde,hydrocinnamaldehyde (3-phenylpropanal, 3-phenylpropionaldehyde),Intreleven aldehyde (undec-10-en-1-al), Ligustral, Trivertal(2,4-dimethyl-3-cyclohexene-1-carboxaldehyde), Jasmorange, satinaldehyde(2-methyl-3-tolylproionaldehyde, 4-dimethylbenzeneprop anal), Lyral(4-(4-hydroxy-4-methyl pentyl)-3-cyclohexene-1-carboxaldehyde), Melonal(2,6-Dimethyl-5-Heptenal), Methoxy Melonal(6-methoxy-2,6-dimethylheptanal), methoxycinnamaldehyde(trans-4-methoxycinnamaldehyde), Myrac aldehyde isohexenylcyclohexenyl-carboxaldehyde, trifernal ((3-methyl-4-phenyl propanal,3-phenyl butanal), lilial, P.T. Bucinal, lysmeral, benzenepropanal(4-tert-butyl-alpha-methyl-hydrocinnamaldehyde), Dupical,tricyclodecylidenebutanal (4-Tricyclo5210-2,6decylidene-8butanal),Melafleur (1,2,3,4,5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde),Methyl Octyl Acetaldehyde, aldehyde C-11 MOA (2-methyl deca-1-al),Onicidal (2,6,10-trimethyl-5,9-undecadien-1-al), Citronellyloxyacetaldehyde, Muguet aldehyde 50 (3,7-dimethyl-6-octenyl)oxyacetaldehyde), phenylacetaldehyde, Mefranal (3-methyl-5-phenylpentanal), Triplal, Vertocitral dimethyl tetrahydrobenzene aldehyde(2,4-dimethyl-3-cyclohexene-1-carboxaldehyde), 2-phenylproprionaldehyde,Hydrotropaldehyde, Canthoxal, anisylpropanal 4-methoxy-alpha-methylbenzenepropanal (2-anisylidene propanal), Cylcemone A(1,2,3,4,5,6,7,8-octahydro-8,8-dimethyl-2-naphthaldehyde), andPrecylcemone B (1-cyclohexene-1-carboxaldehyde).

Still other exemplary aldehydes include, but are not limited to,acetaldehyde (ethanal), pentanal, valeraldehyde, amylaldehyde, Scentenal(octahydro-5-methoxy-4,7-Methano-1H-indene-2-carboxaldehyde),propionaldehyde (propanal), Cyclocitral, beta-cyclocitral,(2,6,6-trimethyl-1-cyclohexene-1-acetaldehyde), Iso Cyclocitral(2,4,6-trimethyl-3-cyclohexene-1-carboxaldehyde), isobutyraldehyde,butyraldehyde, isovaleraldehyde (3-methyl butyraldehyde),methylbutyraldehyde (2-methyl butyraldehyde, 2-methyl butanal),Dihydrocitronellal (3,7-dimethyl octan-1-al), 2-Ethylbutyraldehyde,3-Methyl-2-butenal, 2-Methylpentanal, 2-Methyl Valeraldehyde, Hexenal(2-hexenal, trans-2-hexenal), Heptanal, Octanal, Nonanal, Decanal,Lauric aldehyde, Tridecanal, 2-Dodecanal, Methylthiobutanal,Glutaraldehyde, Pentanedial, Glutaric aldehyde, Heptenal, cis ortrans-Heptenal, Undecenal (2-, 10-), 2,4-octadienal, Nonenal (2-, 6-),Decenal (2-, 4-), 2,4-hexadienal, 2,4-Decadienal, 2,6-Nonadienal,Octenal, 2,6-dimethyl 5-heptenal, 2-isopropyl-5-methyl-2-hexenal,Trifernal, beta methyl Benzenepropanal,2,6,6-Trimethyl-1-cyclohexene-1-acetaldehyde, phenyl Butenal (2-phenyl2-butenal), 2.Methyl-3(p-isopropylphenyl)-propionaldehyde,3-(p-isopropylphenyl)-propionaldehyde, p-Tolylacetaldehyde(4-methylphenylacetaldehyde), Anisaldehyde (p-methoxybenzene aldehyde),Benzaldehyde, Vernaldehyde(1-Methyl-4-(4-methylpentyl)-3-cyclohexenecarbaldehyde), Heliotropin(piperonal) 3,4-Methylene dioxy benzaldehyde, alpha-Amylcinnamicaldehyde, 2-pentyl-3-phenylpropenoic aldehyde, Vanillin (4-methoxy3-hydroxy benzaldehyde), Ethyl vanillin (3-ethoxy4-hydroxybenzaldehyde), Hexyl Cinnamic aldehyde, Jasmonal H(alpha-n-hexyl-cinnamaldehyde), Floralozone,(para-ethyl-alpha,alpha-dimethyl Hydrocinnamaldehyde), Acalea(p-methyl-alpha-pentylcinnamaldehyde), methylcinnamaldehyde,alpha-Methylcinnamaldehyde (2-methyl 3-pheny propenal),alpha-hexylcinnamaldehyde (2-hexyl 3-phenyl propenal), Salicylaldehyde(2-hydroxy benzaldehyde), 4-ethyl benzaldehyde, Cuminaldehyde(4-isopropyl benzaldehyde), Ethoxybenzaldehyde,2,4-dimethylbenzaldehyde, Veratraldehyde (3,4-dimethoxybenzaldehyde),Syringaldehyde (3,5-dimethoxy 4-hydroxybenzaldehyde), Catechaldehyde(3,4-dihydroxybenzaldehyde), Safranal (2,6,6-trimethyl-1,3-dienemethanal), Myrtenal (pin-2-ene-1-carbaldehyde), PerillaldehydeL-4(1-methylethenyl)-1-cyclohexene-1-carboxaldehyde),2,4-Dimethyl-3-cyclohexene carboxaldehyde, 2-Methyl-2-pentenal,2-methylpentenal, pyruvaldehyde, formyl Tricyclodecan, Mandarinaldehyde, Cyclemax, Pino acetaldehyde, Corps Iris, Maceal, and Corps4322.

In one embodiment, the malodor control composition includes a mixture oftwo or more volatile aldehydes selected from the group consisting of2-ethoxy Benzylaldehyde, 2-isopropyl-5-methyl-2-hexenal, 5-methylFurfural, 5-methyl-thiophene-carboxaldehyde, Adoxal, p-anisaldehyde,Benzylaldehyde, Bourgenal, Cinnamic aldehyde, Cymal, Decyl aldehyde,Floral super, Florhydral, Helional, Lauric aldehyde, Ligustral, Lyral,Melonal, o-anisaldehyde, Pino acetaldehyde, P.T. Bucinal, Thiophenecarboxaldehyde, trans-4-Decenal, trans trans 2,4-Nonadienal, Undecylaldehyde, and mixtures thereof.

In some embodiments, the malodor control composition includes fastreacting volatile aldehydes. “Fast reacting volatile aldehydes” refersto volatile aldehydes that either (1) reduce amine odors by 20% or morein less than 40 seconds; or (2) reduce thiol odors by 20% or more inless than 30 minutes.

In one embodiment, the malodor control composition includes a mixture ofthe volatile aldehydes listed in Table 1 and referred to herein asAccord A.

TABLE 1 Accord A ClogP VP(torr) Material Wt. % CAS Number Group @25° C.Intreleven Aldehyde 5.000 112-45-8 3 0.060 Florhydral 10.000 125109-85-54 0.008 Floral Super 25.000 71077-31-1 3 0.030 Scentenal 10.00086803-90-9 2 0.010 Cymal 25.000 103-95-7 4 0.007 o-anisaldehyde 25.000135-02-4 1 0.032

In another embodiment, the malodor control composition includes amixture of the volatile aldehydes listed in Table 2 and referred toherein as Accord B.

TABLE 2 Accord B ClogP VP (torr) Material Wt. % CAS Number Group @25° C.Intreleven Aldehyde 2.000 112-45-8 3 0.060 Florhydral 20.000 125109-85-54 0.008 Floral Super 10.000 71077-31-1 3 0.030 Scentenal 5.00086803-90-9 2 0.010 Cymal 25.000 103-95-7 4 0.007 Floralozone 10.00067634-14-4 4 0.005 Adoxal 1.000 141-13-9 4 0.007 Methyl Nonyl 1.000110-41-8 3 0.030 Acetaldehyde Melonal 1.000 106-72-9 3 0.670o-anisaldehyde 25.000 135-02-4 1 0.032

In another embodiment, the malodor control composition includes amixture of about 71.2% volatile aldehydes, the remainder being other anester and an alcohol perfume raw material. This mixture is listed inTable 3 and referred to herein as Accord C.

TABLE 3 Accord C ClogP VP (torr) Material Wt. % CAS Number Group @25° C.Intreleven Aldehyde 2.000 112-45-8 3 0.060 Florhydral 10.000 125109-85-54 0.008 Floral Super 5.000 71077-31-1 3 0.030 Scentenal 2.000 86803-90-92 0.010 Cymal 15.000 103-95-7 4 0.007 Floralozone 12.000 67634-14-4 40.005 Adoxal 1.000 141-13-9 4 0.007 Methyl Nonyl 1.000 110-41-8 3 0.030Acetaldehyde Melonal 1.000 106-72-9 3 0.670 Flor Acetate 11.8005413-60-5 1 0.060 Frutene 7.000 17511-60-3 4 0.020 Helional 5.0001205-17-0 2 0.0005 Bourgeonal 2.000 18127-01-0 4 0.004 Linalool 10.00078-70-6 3 0.050 Benzaldehyde 0.200 100-52-7 1 1.110 o-anisaldehyde15.000 135-02-4 1 0.320

Accords A, B, or C can be formulated in with other perfume raw materialsin an amount, for example, of about 10% by weight of the malodor controlcomposition. Additionally, the individual volatile aldehydes or avarious combination of the volatile aldehydes can be formulated into amalodor control composition. In certain embodiments, the volatilealdehydes may be present in an amount up to 100%, by weight of themalodor control composition, alternatively from about 0.1% to about100%, alternatively from about 1% to about 100%, alternatively fromabout 2% to about 100%, alternatively from about 3% to about 100%,alternatively about 50% to about 100%, alternatively about 70% to about100%, alternatively about 80% to about 100%, alternatively from about 1%to about 20%, alternatively from about 0.1% to about 10%, alternativelyfrom about 1% to about 10%, alternatively from about 0.1% to about 5%,alternatively from about 1% to about 5%, alternatively from about 1% toabout 3%, alternatively from about 2% to about 20%, alternatively fromabout 3% to about 20%, alternatively from about 4% to about 20%,alternatively from about 5% to about 20%, by weight of the composition.

In some embodiments where volatility is not important for neutralizing amalodor, the present invention may include poly-aldehydes, for example,di-, tri-, tetra-aldehydes. Such embodiments may include laundrydetergents, additive, and the like for leave-on, through the wash, andrinse-off type of applications.

2. Acid Catalyst

The malodor control composition of the present invention may include aneffective amount of an acid catalyst to neutralize sulfur-basedmalodors. It has been found that certain mild acids have an impact onaldehyde reactivity with thiols in the liquid and vapor phase. It hasbeen found that the reaction between thiol and aldehyde is a catalyticreaction that follows the mechanism of hemiacetal and acetal formationpath. When the present malodor control composition contains an acidcatalyst and contacts a sulfur-based malodor, the volatile aldehydereacts with thiol. This reaction may form a thiol acetal compound, thus,neutralizing the sulfur-based odor. Without an acid catalyst, onlyhemi-thiol acetal is formed.

Suitable acid catalysts have a VP, as reported by Scifinder, in therange of about 0.001 torr to about 38 torr, measured at 25° C.,alternatively about 0.001 torr to about 14 torr, alternatively fromabout 0.001 to about 1, alternatively from about 0.001 to about 0.020,alternatively about 0.005 to about 0.020, alternatively about 0.010 toabout 0.020.

The acid catalyst may be a weak acid. A weak acid is characterized by anacid dissociation constant, Ka, which is an equilibrium constant for thedissociation of a weak acid; the pKa being equal to minus the decimallogarithm of Ka. The acid catalyst may have a pKa from about 4.0 toabout 6.0, alternatively from about 4.3 and 5.7, alternatively fromabout 4.5 to about 5, alternatively from about 4.7 to about 4.9.Suitable acid catalyst include those listed in Table 4.

TABLE 4 VP (torr) Material @ 25° C. Formic Acid 36.5 Acetic Acid 13.9Trimethyl Acetic Acid 0.907 Phenol (alkaline in liquid apps yet 0.610acidic in vapor phase) Tiglic acid 0.152 Caprylic acid 0.0222 5-Methylthiophene carboxylic acid 0.019 Succinic acid 0.0165 Benzoic acid 0.014Mesitylenic acid 0.00211

Depending on the desired use of the malodor control composition, one mayconsider the scent character or the affect on the scent of the malodorcontrol composition when selecting an acid catalyst. In some embodimentsof the malodor control composition, it may be desirable to select anacid catalyst that provides a neutral to pleasant scent. Such acidcatalysts may have a VP of about 0.001 torr to about 0.020 torr,measured at 25° C., alternatively about 0.005 torr to about 0.020 torr,alternatively about 0.010 torr to about 0.020 torr. Non-limitingexamples of such acid catalyst include 5-methyl thiophene carboxaldehydewith carboxylic acid impurity, succinic acid, or benzoic acid.

The malodor control composition may include about 0.01% to about 5%,alternatively about 0.04% to about 1.5%, alternatively about 0.1% toabout 1.0%, alternatively about 0.1% to about 0.5%, alternatively about0.01% to about 0.4%, alternatively about 0.1% to about 0.4%,alternatively about 0.04% to about 1.5%, alternatively about 0.4% of anacid catalyst by weight of the malodor control composition.

In an acetic acid system, the present malodor control composition mayinclude about 0.4% of acetic acid (50:50 TC:DPM, 0.4% acetic acid).

TABLE 5 % Butanethiol Actual % acetic reduction @ Sample Formulated acidin DPM 30 min. 50:50 TC:DPM 0% Acetic Acid 0.00 12.00 50:50 TC:DPM 0.05%Acetic Acid 0.04 14.65 50:50 TC:DPM 0.1% Acetic Acid 0.10 25.66 50:50TC:DPM 0.2% Acetic Acid 0.42 34.68 50:50 TC:DPM 0.5% Acetic Acid 1.0024.79 50:50 TC:DPM 1.0% Acetic Acid 2.00 7.26

When an acid catalyst is present with a volatile aldehyde (or RA), theacid catalyst may increase the efficacy of the volatile aldehyde onmalodors in comparison to the malodor efficacy of the volatile aldehydeon its own. For example, 1% volatile aldehyde and 1.5% benzoic acidprovides malodor removal benefit equal to or better than 5% volatilealdehyde alone.

The malodor control composition may have a pH from about 3 to about 8,alternatively from about 4 to about 7, alternatively from about,alternatively from about 4 to about 6.

3. Optional Ingredients

The malodor control composition may, optionally, include odor maskingagents, odor blocking agents, and/or diluents. For example, the malodorcontrol composition may include a mixture of volatile aldehydes forneutralizing a malodor, perfume ionones, and a diluent. Alternatively,the malodor control composition may include 100% volatile aldehydes.

“Odor-masking agents” refer to known compounds (e.g. perfume rawmaterials) that mask or hide a malodorous compound. Odor-masking mayinclude a compound with a non-offensive or pleasant smell that is dosedsuch it limits the ability to sense a malodorous compound. Odor-maskingmay involve the selection of compounds which coordinate with ananticipated malodor to change the perception of the overall scentprovided by the combination of odorous compounds.

“Odor blocking agents” refer to known compounds that dull the humansense of smell.

Exemplary diluents include dipropylene glycol methyl ether, and3-methoxy-3-methyl-1-butanol, and mixtures thereof.

The malodor control composition may also, optionally, include perfumeraw materials that solely provide a hedonic benefit (i.e. that do notneutralize malodors yet provide a pleasant fragrance). Suitable perfumesare disclosed in U.S. Pat. No. 6,248,135, which is incorporated in itsentirety by reference.

III. Method of Use

The malodor control composition of the present invention may be used ina wide variety of applications that neutralize malodors in the vaporand/or liquid phase. The malodor control composition may be formulatedfor use in substrates such as plastics, wovens, or non-wovens (e.g.cellulose fibers for paper products). Such substrates may be used as petfood packaging; paper towels; tissues; trash bags; diapers, toddlertraining pants; baby wipes; adult incontinence products; femininehygiene products such as sanitary napkins and tampons.

In particular, the present invention encompasses a method ofneutralizing malodor associated with urine, menses, and/or feces,comprising contacting said malodor with the absorbent article comprisingthe malodor control composition of the present invention. Examples ofsuitable absorbent articles include diapers, toddler training pants,adult incontinence garments, sanitary napkins, pantiliners, interlabialdevices, hemorrhoid pads, and the like.

EXAMPLES Analytical Test Effect of Volatile Aldehydes on Amine-Based andSulfur-Based Malodors

Malodor standards are prepared by pipeting 1 mL of butylamine(amine-based malodor) and butanethiol (sulfur-based malodor) into a 1.2liter gas sampling bag. The bag is then filled to volume with nitrogenand allowed to sit for at least 12 hours to equilibrate.

A 1 μL sample of each volatile aldehyde listed in Table 6 and of eachAccord (A, B, and C) listed in Tables 1 to 3 is pipeted into individual10 mL silanized headspace vials. The vials are sealed and allowed toequilibrate for at least 12 hours. Repeat 4 times for each sample (2 forbutylamine analysis and 2 for butanethiol analysis).

After the equilibration period, 1.5 mL of the target malodor standard isinjected into each 10 mL vial. For thiol analysis, the vials containinga sample +malodor standard are held at room temperature for 30 minutes.Then, a 1 mL headspace syringe is then used to inject 250 μL of eachsample/malodor into a GC/MS split/splitless inlet. For amine analysis, a1 mL headspace syringe is used to inject 500 μL of each sample/malodorimmediately into the GC/MS split/splitless inlet. A GC pillow is usedfor the amine analysis to shorten the run times.

Samples are then analyzed using a GC/MS with a DB-5, 20 m, 1 μm filmthickness column with an MPS-2 autosampler equipment with staticheadspace function. Data is analyzed by ion extraction on each total ioncurrent (56 for thiol and 30 for amine) and the area is used tocalculate the percent reduction from the malodor standard for eachsample.

Table 6 shows the effect of certain volatile aldehydes on neutralizingamine-based and sulfur based malodors at 40 seconds and 30 minutes,respectively.

TABLE 6 At least 20% At least 20% butylamine butanethiol reduction at 40reduction at 30 Perfume Raw Material (R—CHO) secs.? mins.? 2,4,5Trimethoxy Benzaldehyde No No 2,4,6-Trimethoxy-benzylaldehyde No No2-ethoxy benzylaldehyde Yes Yes 2-isopropyl-5-methyl-2-hexenal Yes Yes2-methyl-3-(2-furyl)-propenal No No 3,4,5 Trimethoxy Benzaldehyde No No3,4-Trimethoxy-benzylaldehyde No No 4-tertbutyl benzylaldehyde Yes No5-methyl furfural Yes Yes 5-methyl-thiophene-carboxaldehyde No YesAdoxal Yes No Amyl cinnamic aldehyde No No Benzylaldehyde Yes NoBourgenal No Yes Cinnamic aldehyde Yes Yes Citronelyl Oxyacetaldehyde NoNo Cymal Yes No Decyl aldehyde Yes No Floral Super Yes Yes FlorhydralYes Yes Floralozone No No Helional Yes No Hydroxycitronellal No NoLauric aldehyde Yes No Ligustral Yes No Lyral Yes No Melonal Yes NoMethyl nonyl acetaldehyde No No o-anisaldehyde Yes Yes p-anisaldehydeYes No Pino acetaldehyde Yes Yes P.T. Bucinal Yes No ThiopheneCarboxaldehyde Yes No Trans-4-decenal Yes Yes Trans Trans 2,4-NonadienalYes No Undecyl aldehyde Yes No

Table 7 shows the percent reduction of butylamine and butanethiol at 40seconds and 30 minutes, respectively, for Accords A, B, and C.

TABLE 7 % reduction of butylamine % reduction of butanethiol Accord at40 secs. at 30 mins. Accord A 76.58 25.22 Accord B 51.54 35.38 Accord C65.34 24.98Analytical Test—Effect Of Acid Catalysts On Sulfur-Based Malodors

The above analytical test is repeated using samples containing an acidcatalyst to test their effect on sulfur-based malodors. Specifically, a1 μL aliquot of each of the following controls and acid catalyst samplesare pipeted into individual 10 mL silanized headspace vials induplicate: thiophene carboxyaldehyde as a control; a 50/50 mixture ofthiophene carboxaldehyde and each of the following acid catalysts at0.04%, 0.10%, 0.43% in DPM, 1.02% in DPM, and 2.04% in DPM: phenol,mesitylenic acid, caprylic acid, succinic acid, pivalic acid, tiglicacid, and benzoic acid.

FIG. 1 demonstrates that low vapor pressure acid catalysts provide up to3 times better reduction of sulfur-based malodors in comparison to thecontrol.

Analytical Test—Effect Of Volatile Aldehydes And Acid Catalyst OnAmine-Based And Sulfur-Based Malodors

The above analytical test is repeated using sample formulationscontaining volatile aldehydes (or RA) and an acid catalyst, as outlinedin Tables 8 and 9.

Tables 8 and 9 show that a perfume mixture having as little as 1%volatile aldehyde along with 1.5% acid catalyst performs better atreducing butylamine and butanethiol than the same perfume mixture having5% volatile aldehyde.

TABLE 8 % butylamine reduction % butanethiol reduction Formulation at 40secs. at 30 mins. Perfume Mixture 34.21 — 2.40 — w/5% RA (Control)Perfume Mixture 41.63 +7.42 11.95 +9.55 w/1% RA and w/ 1.5% Benzoic AcidPerfume Mixture 36.19 +1.98 13.56 +11.16 w/3% RA and w/ 1.5% BenzoicAcid Perfume A Mixture 41.26 +7.05 9.56 +5.02 w/5% RA and w/ 1.5%Benzoic Acid

TABLE 9 % butylamine Reduction % butanethiol reduction Formulation at 40secs. at 30 mins. Perfume mixture 4.94 — 10.52 — w/5% RA (Control)Perfume mixture 11.61 +6.67 18.82 +8.30 w/1% RA and w/ 1.5% Benzoic AcidPerfume mixture 26.89 +21.95 14.85 +4.33 w/3% RA and w/ 1.5% BenzoicAcid Perfume mixture 20.27 +15.33 16.84 +6.32 w/5% RA and w/ 1.5%Benzoic Acid

The dimensions and values disclosed herein are not to be understood asbeing strictly limited to the exact numerical values recited. Instead,unless otherwise specified, each such dimension is intended to mean boththe recited value and a functionally equivalent range surrounding thatvalue. For example, a dimension disclosed as “40 mm” is intended to mean“about 40 mm.”

Every document cited herein, including any cross referenced or relatedpatent or application, is hereby incorporated herein by reference in itsentirety unless expressly excluded or otherwise limited. The citation ofany document is not an admission that it is prior art with respect toany invention disclosed or claimed herein or that it alone, or in anycombination with any other reference or references, teaches, suggests,or discloses any such invention. Further, to the extent that any meaningor definition of a term in this document conflicts with any meaning ordefinition of the same term in a document incorporated by reference, themeaning or definition assigned to that term in this document shallgovern.

While particular embodiments of the present invention have beenillustrated and described, it would be obvious to those skilled in theart that various other changes and modifications can be made withoutdeparting from the spirit and scope of the invention. It is, therefore,intended to cover in the appended claims all such changes andmodifications that are within the scope of this invention.

What is claimed:
 1. An absorbent article comprising a malodor controlcomposition disposed therein, said malodor control compositioncomprising: at least one volatile aldehyde; an acid catalyst having avapor pressure of about 0.01 to about 13 at 25° C.; wherein said atleast one volatile aldehyde is present in an amount from about 0.1% toabout 5%, by weight of said malodor control composition, and said acidcatalyst is present in an amount of about 0.1% to about 1%, by weight ofsaid malodor control composition.
 2. The absorbent article of claim 1wherein said at least one volatile aldehyde has a VP of about 0.001 toabout 50 torr.
 3. The absorbent article of claim 1 wherein said at leastone volatile aldehyde has a VP of about 0.001 torr to about 15 torr. 4.The absorbent article of claim 1 wherein said at least one volatilealdehyde is selected from the group consisting of 2-ethoxybenzylaldehyde, 2-isopropyl-5-methyl-2-hexenal, 5-methyl furfural,5-methyl-thiophene-carboxaldehyde, adoxal, p-anisaldehyde,benzylaldehyde, bourgenal, cinnamic aldehyde, cymal, decyl aldehyde,floral super, florhydral, helional, lauric aldehyde, ligustral, lyral,melonal, o-anisaldehyde, pino acetaldehyde, P.T. bucinal, thiophenecarboxaldehyde, trans-4-decenal, trans trans 2,4-nonadienal, undecylaldehyde, and mixtures thereof.
 5. The absorbent article of claim 1wherein said at least one volatile aldehyde is selected from the groupconsisting of flor super, o-anisaldehyde, and mixtures thereof.
 6. Theabsorbent article of claim 1 wherein said at least one volatile aldehydecomprises a mixture of volatile aldehydes selected from the groupconsisting of Intreleven Aldehyde, Florhydral,4,8.dimethyl-4,9.decadienal, Scentenal, Cymal, o-anisaldehyde,Floralozone, Adoxal, Methyl Nonyl Acetaldehyde, Melonal, Flor Acetate,Frutene, Helional, Bourgeonal, Linalool, Benzaldehyde, and mixturesthereof.
 7. The absorbent article of claim 1 wherein said at least onevolatile aldehyde comprises a mixture of volatile aldehydes, saidmixture comprising about 0.1% to about 10% of Accord A, by weight ofsaid malodor control composition; wherein Accord A comprises 5% byweight of Intreleven Aldehyde, 10% by weight of Florhydral, 25% byweight of 4,8.dimethyl-4,9.decadienal, 10% by weight of Scentenal, 25%by weight of Cymal, and 25% by weight o-anisaldehyde.
 8. The absorbentarticle of claim 1 wherein said acid catalyst has a vapor pressure ofabout 0.01 to about 2 torr at 25° C.
 9. The absorbent article of claim 1wherein said acid catalyst is a carboxylic acid.
 10. The absorbentarticle of claim 1 wherein said acid catalyst is present in an amountfrom about 0.01% to about 0.4%, by weight of said malodor controlcomposition.
 11. The absorbent article of claim 1 wherein said acidcatalyst is present in an amount of about 0.4%, by weight of saidmalodor control composition.
 12. The absorbent article of claim 1wherein said composition has a pH of about 4 to about 6.5.
 13. Theabsorbent article of claim 1 further comprising an ingredient selectedfrom the group consisting of: odor masking agents, odor blocking agents,diluents, and mixtures thereof.
 14. The absorbent article of claim 1,wherein said absorbent article is selected from the group consisting ofa diaper, an adult incontinence garment, a sanitary napkin, apantiliner, an interlabial device, and a hemorrhoid pad.
 15. Theabsorbent article of claim 1, wherein said absorbent article furthercomprises a topsheet, a backsheet, and an absorbent core disposedbetween said topsheet and said backsheet.
 16. The absorbent article ofclaim 15, wherein said absorbent core has a garment-facing side and abody-facing side, and wherein said malodor control composition isdisposed on said garment-facing side of said absorbent core.
 17. Amethod of neutralizing malodor associated with urine, menses, and/orfeces, comprising contacting said malodor with the absorbent article ofclaim 1.